Stevenage, Hertfordshire, South East, United Kingdom
Russell Taylor Group Ltd
tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPAand change control for which you are the owner are progressed in a compliant and timely manner and all other items are reviewed and/or approved in accordance with … hold a degree in a STEM related subject Experienced in batch review and batch release GMP QA experience is essential! Ideally in a Pharmaceutical setting or similar Experience in CAPA, deviations, change controls, internal auditing (preferred) etc Strong interpersonal skills, we are looking for Candidates who are good communicators Strong written and verbal use of English language essential due to More ❯
development of organizational strategies by aligning quality and compliance with company goals - Sign off on deliverables as per the approval matrix - Support and guide the team in ongoing development, CAPA/NC activities, training tracking, RFx responses, and continuous improvement activities - Act as the Management Representative and oversee Management Review meetings Skills - Experienced professional with a strong understanding of transforming More ❯
primary contact with regard to Quality performance Administer the Fault Analysis Reporting process and ensure that the reports are distributed to management and monitor the completion of the correctiveandpreventiveaction of each entry. Manage the internal and external audit process and assist with audits where appropriate and/or necessary. To ensure that the Quality Systems are harmonised More ❯
team ? Exceptional benefits and career development ?? Key Responsibilities: Accreditation & Compliance Maintain ISO9001, ISO13485, ISO18001, ISO14001, and ISO45001 standards Conduct internal and external audits Ensure REACH and ROHS compliance Manage CAPAand document control systems Quality Control Improve manufacturing quality controls to reduce defects and costs Manage supplier performance and customer returns Implement corrective actions to enhance customer satisfaction Customer Support More ❯
Leighton Buzzard, Bedfordshire, South East, United Kingdom
1TECH STAFFING LIMITED
and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting audits (regulatory, ISO, client, supplier) and managing CAPA plans. Driving a culture of quality excellence across the business. Conducting supplier audits, internal inspections, and management reviews. Key Requirements: Proven experience in a GMDP or similar regulated environment. Strong More ❯
levels to ensure traceability. Identify, segregate, and document non-conforming products, and support Quality and Operation teams to resolve quality issues. Assist in root cause investigations and support correctiveandpreventiveaction processes. Maintain a clean and organised inspection area maintaining appropriate H&S standards. Update the company’s ERP system with accurate and timely quality data, including inspection results More ❯
to recommend service improvements. Work with ITSM teams to ensure accurate SLA tracking and OLA performance reporting within ServiceNow. Support the definition and implementation of correctiveandpreventive actions (CAPA) based on insights. Develop and manage automated and custom reports from ServiceNow Performance Analytics, ServiceNow Reporting, and other BI platforms (e.g., Power BI) Create real-time dashboards to monitor IT More ❯